Canonical Allele Identifier: CA393309531

Gene: AP3B2 CPEB1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.83331913C>T (hg19) ; chr15:g.82663161C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82663161C>T , CM000677.2:g.82663161C>T	GRCh38
NC_000015.9:g.83331913C>T , CM000677.1:g.83331913C>T	GRCh37
NC_000015.8:g.81128968C>T	NCBI36
NG_052957.1:g.51748G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261722.8:c.2531G>A (AP3B2)	ENSP00000261722.4:p.Gly844Asp
ENST00000535359.6:c.2570G>A (AP3B2) MANE Select	ENSP00000440984.1:p.Gly857Asp
ENST00000535385.6:n.3016G>A (AP3B2)
ENST00000537735.2:n.2659G>A (AP3B2)
ENST00000543938.6:n.2716G>A (AP3B2)
ENST00000642989.2:c.2642G>A (AP3B2)	ENSP00000493485.1:p.Gly881Asp
ENST00000652847.1:c.2513G>A (AP3B2)	ENSP00000499785.1:p.Gly838Asp
ENST00000657321.1:c.*2588G>A (AP3B2)	ENSP00000499716.1:n.*2588G>A
ENST00000660624.1:c.1421G>A (AP3B2)	ENSP00000499379.1:p.Gly474Asp
ENST00000661532.1:c.1802G>A (AP3B2)
ENST00000663651.1:n.2655G>A (AP3B2)
ENST00000666973.1:c.2513G>A (AP3B2)	ENSP00000499288.1:p.Gly838Asp
ENST00000667758.1:c.*2727G>A (AP3B2)	ENSP00000499318.1:n.*2727G>A
ENST00000668385.1:c.*2311G>A (AP3B2)	ENSP00000499544.1:n.*2311G>A
ENST00000668458.1:c.2261G>A (AP3B2)
ENST00000668990.2:c.2513G>A (AP3B2)	ENSP00000499235.1:p.Gly838Asp
ENST00000669930.1:c.2342G>A (AP3B2)	ENSP00000499671.1:p.Gly781Asp
ENST00000679388.1:n.2452G>A (AP3B2)
ENST00000679531.1:n.2919G>A (AP3B2)
ENST00000679891.1:n.950G>A (AP3B2)
ENST00000679950.1:n.3218G>A (AP3B2)
ENST00000680492.1:n.3552G>A (AP3B2)
ENST00000680912.1:n.1489G>A (AP3B2)
ENST00000680946.1:n.2919G>A (AP3B2)
ENST00000681044.1:n.3425G>A (AP3B2)
ENST00000681327.1:c.*2588G>A (AP3B2)	ENSP00000505423.1:n.*2588G>A
ENST00000681452.1:n.2919G>A (AP3B2)
ENST00000681464.1:n.3425G>A (AP3B2)
ENST00000261722.7:c.2513G>A (AP3B2)	ENSP00000261722.3:p.Gly838Asp
ENST00000535348.5:c.2417G>A (AP3B2)	ENSP00000438721.1:p.Gly806Asp
ENST00000535359.5:c.2570G>A (AP3B2)	ENSP00000440984.1:p.Gly857Asp
ENST00000538592.1:c.160G>A (AP3B2)	ENSP00000445804.1:n.160G>A
ENST00000543938.5:n.1636G>A (AP3B2)
ENST00000545315.1:n.89G>A (AP3B2)
ENST00000620652.4:c.2513G>A (AP3B2)	ENSP00000479229.1:p.Gly838Asp
NM_001278511.1:c.2417G>A (AP3B2)	NP_001265440.1:p.Gly806Asp
NM_001278512.1:c.2570G>A (AP3B2)	NP_001265441.1:p.Gly857Asp
NM_004644.4:c.2513G>A (AP3B2)	NP_004635.2:p.Gly838Asp
NR_046096.1:n.1328+13015C>T (CPEB1-AS1)
XM_011522097.1:c.2498G>A (AP3B2)	XP_011520399.1:p.Gly833Asp
XM_011522098.1:c.2474G>A (AP3B2)	XP_011520400.1:p.Gly825Asp
XM_011522100.1:c.1421G>A (AP3B2)	XP_011520402.1:p.Gly474Asp
XM_017022640.2:c.2441G>A (AP3B2)	XP_016878129.1:p.Gly814Asp
XM_024450081.1:c.-149G>A (AP3B2)	XP_024305849.1:n.-149G>A
XM_024450082.1:c.-740G>A (AP3B2)	XP_024305850.1:n.-740G>A
XR_001751404.2:n.2741G>A (AP3B2)
NM_001278512.2:c.2570G>A (AP3B2) MANE Select	NP_001265441.1:p.Gly857Asp
NM_004644.5:c.2513G>A (AP3B2)	NP_004635.2:p.Gly838Asp
NM_001278511.2:c.2417G>A (AP3B2)	NP_001265440.1:p.Gly806Asp